ライフサイエンスコーパス: supplementary motor area

1 tive conditions increased activations in the supplementary motor area.

2 ight lateral prefrontal cortex and bilateral supplementary motor area.

3 classified more reliably, especially in the supplementary motor area.

4 (VLPFC)/insula, inferior frontal cortex, and supplementary motor area.

5 s region with the anterior cingulate and pre-supplementary motor area.

6 ecially between the primary motor cortex and supplementary motor area.

7 ophy of superior lateral premotor cortex and supplementary motor area.

8 anatomical bundle, and overlapping with the supplementary motor area.

9 nd thalamus, and increased activation in the supplementary motor area.

10 coactivation of the primary motor cortex and supplementary motor area.

11 cal motor scores and brain metabolism in the supplementary motor area.

12 connectivity between anterior cingulate and supplementary motor area.

13 ion in beta power in the premotor cortex and supplementary motor area.

14 neuron activity was recorded from the caudal supplementary motor area.

15 e primary motor cortex than with that of the supplementary motor area.

16 ing Broca's area, the premotor area, and the supplementary motor area.

17 esial premotor areas, probably including the supplementary motor area.

18 ), the lateral premotor cortex and bilateral supplementary motor area.

19 l cortex and cerebellum, and medially in the supplementary motor area.

20 p received 15 sessions of 1-Hz rTMS over the supplementary motor area.

21 d the thalamus, habenula, mid-cingulate, and supplementary motor area.

22 he ventral PMC and the dorsal portion of the supplementary motor area.

23 tex, central operculum/posterior insula, and supplementary motor area.

24 y within the dACC and spreading into the pre-supplementary motor area.

25 cific locus at the ventral border of the pre-supplementary motor area.

26 mporary goals, which may be monitored by the supplementary motor area.

27 ion in beta power in the premotor cortex and supplementary motor area.

28 y be due to disconnection from cingulate and supplementary motor areas.

29 ity in the lentiform nuclei, cerebellum, and supplementary motor areas.

30 ing Broca's area as well as the premotor and supplementary motor areas.

31 emotor, dorsolateral prefrontal and anterior supplementary motor areas.

32 s and mesial premotor regions, including the supplementary motor areas.

33 Fifteen sessions of rTMS in 3 weeks over the supplementary motor area: 1-Hz rTMS, iTBS, sham, or no t

34 y reduced neural response to laughter in the supplementary motor area, a premotor region thought to f

35 We argue here for the engagement of supplementary motor areas across a variety of sound cate

36 All patients showed greater relative supplementary motor area activation than did the normal

37 maging, MC4R agonism enhanced cerebellar and supplementary motor area activity and deactivated the se

38 Furthermore, supplementary motor area activity drove STN activity sel

39 ve ipsilateral premotor cortex and bilateral supplementary motor area activity.

40 lism of superior lateral premotor cortex and supplementary motor area, although there was some variab

41 ding the left and right presupplementary and supplementary motor area and anterior cingulate cortex.

42 e temporal cortex, and medial regions in the supplementary motor area and anterior cingulate.

43 e inhibition meta-analysis, showing that the supplementary motor area and basal ganglia were underact

44 g the primary motor cortex, premotor cortex, supplementary motor area and basal ganglia.

45 nnectivity between amygdala and motor areas (supplementary motor area and cerebellum) was enhanced.

46 sensorimotor cortex, dorsal premotor cortex, supplementary motor area and cerebellum.

47 erses, at least partially, the impairment of supplementary motor area and dorsal prefrontal cortex ac

48 ed that it would also concomitantly increase supplementary motor area and dorsal prefrontal cortex ac

49 fects for two medial frontal brain regions - supplementary motor area and frontal polar cortex.

50 esponse including structural connectivity to supplementary motor area and functional anticorrelation

51 The supplementary motor area and inferior frontal cortex act

52 al primary sensorimotor and premotor cortex, supplementary motor area and ipsilateral cerebellar cort

53 BOLD activation in right premotor cortex and supplementary motor area and left hippocampus and with i

54 lysis, our results suggest motor output from supplementary motor area and left primary motor cortex a

55 ied to the scalp overlying the region of the supplementary motor area and over other positions, inclu

56 ctional connectivity at rest between the pre-supplementary motor area and prefrontal cortex were prop

57 Supplementary motor area and premotor cortex had spectra

58 The sequence of activation suggests that supplementary motor area and premotor cortex interrupted

59 The results also showed that supplementary motor area and putamen/globus pallidus reg

60 Supplementary motor area and right dorsal prefrontal cor

61 Relative increases in activation of the supplementary motor area and right dorsal prefrontal cor

62 Coherence between supplementary motor area and STN within the high (21-30

63 re condition, accompanied by increased right supplementary motor area and temporoparietal junction ac

64 ptom-related motor planning and body schema (supplementary motor area and temporoparietal junction).

65 arietal lobules, the frontal eye fields, the supplementary motor area and the anterior insulae.

66 and recruited more areas, including the pre-supplementary motor area and the bilateral posterior lob

67 A network involving supplementary motor area and the caudal portion of dorsa

68 omponent of this network originates from the supplementary motor area and the cingulate motor areas o

69 ects were associated with connections to the supplementary motor area and the decussating cerebelloth

70 sensorimotor cortex, dorsal premotor cortex, supplementary motor area and the inferior parietal corte

71 d significantly with activations in the left supplementary motor area and the left medial parietal co

72 ht lobe, particularly in regions such as the supplementary motor area and the lingual gyrus.

73 ional connectivity network included the left supplementary motor area and the prefrontal, inferior pa

74 Moreover, foci in the right rostral supplementary motor area and the right inferior parietal

75 The pre-supplementary motor area and the rostral portion of the

76 By contrast, separate signals in supplementary motor area and ventromedial prefrontal cor

77 rturbation-evoked potential localized to the supplementary motor area) and lower sensorimotor beta EE

78 ction), pain processing (anterior insula and supplementary motor area), and identification of emotion

79 left lateral orbitofrontal cortex and right supplementary motor area, and also dissociated abnormali

80 orks, including the inferior frontal cortex, supplementary motor area, and anterior cingulate cortex

81 bition in the right inferior frontal cortex, supplementary motor area, and anterior cingulate cortex,

82 e bilateral putamen, anterior-dorsal insula, supplementary motor area, and anterior cingulate cortex.

83 ontal and parietal cortex, dorsal cingulate, supplementary motor area, and anterior insula.

84 ivity between the vermis 3 and the bilateral supplementary motor area, and between the vermis 4,5 and

85 etwork, including right angular gyrus, right supplementary motor area, and bilateral cerebellum, yiel

86 erior frontal gyrus, left anterior cingulate/supplementary motor area, and bilateral posterior cingul

87 frontal cortex, superior temporal gyrus, and supplementary motor area, and bilaterally in the medial

88 ated to changes in grey matter volume in pre-supplementary motor area, and changes in its underlying

89 A significant proportion of neurons in supplementary motor area, and hippocampus and environs,

90 ITG), left postcentral gyrus/precuneus, left supplementary motor area, and left lingual gyrus were id

91 bilateral dorsal anterior cingulate cortex, supplementary motor area, and pre-supplementary motor ar

92 t hemisphere, including sensorimotor cortex, supplementary motor area, and rostral inferior parietal

93 hibition engages the inferior frontal gyrus, supplementary motor area, and striatum.

94 afferents from the primary motor cortex, the supplementary motor area, and the caudal subdivision of

95 sensorimotor cortex, inferior-frontal gyrus, supplementary motor area, and the cerebellum.

96 zed by hypermetabolism of the basal ganglia, supplementary motor area, and the cerebellum.

97 cortex, the insula bilaterally, the midline supplementary motor area, and the medial parietal cortex

98 eys composed of bilateral premotor cortices, supplementary motor area, and the right inferior frontal

99 , and anterior PFC, lateral premotor cortex, supplementary motor area, and the striatum are involved

100 orsal premotor cortex, supplementary and pre-supplementary motor areas, and planum temporale), b) dom

101 icle (SLF) to dorsal area 6, area 9, and the supplementary motor area; and via the cingulate fascicle

102 lateral premotor area, orbitofrontal cortex, supplementary motor area, anteior cingulate gyrus) and p

103 with significantly reduced activation in the supplementary motor area, anterior cingulate and midcing

104 The supplementary motor area appears important for productio

105 the ventral lateral premotor cortex, and the supplementary motor area are essential for the voluntary

106 ulation (the anterior insula, cerebellum and supplementary motor area) arguably because the reading r

107 te cortex, supplementary motor area, and pre-supplementary motor area as well as right anterior insul

108 ases in the dorsal midbrain, cerebellum, and supplementary motor area, as well as reductions in motor

109 the dorsal anterior cingulate cortex and the supplementary motor area, as well as the insula, which w

110 e superior motor cortex, premotor cortex and supplementary motor area at loci similar to those detect

111 x (Brodmann area [BA] 4), bilaterally in the supplementary motor area (BA 6), and in the right anteri

112 g the anterior cingulate cortex (BA 24), the supplementary motor area (BA 6), and the precuneus, enco

113 organized with a sharp transition around the supplementary motor area between fast (13-15 Hz) centrop

114 f interest, as well as activation within the supplementary motor area, brainstem, and inferior fronta

115 ficantly correlated with the activity of the supplementary motor area but not with that of the primar

116 of the mesial premotor system, including the supplementary motor area, but also by enhancing informat

117 or insula, anterior/mid-cingulate cortex and supplementary motor area, but showed no difference from

118 hin the anterior insula and presupplementary/supplementary motor areas, carried behavioral consequenc

119 ation, including dorsal premotor cortex, pre-supplementary motor area, cerebellum, and basal ganglia

120 led regions of occipital lobe, frontal lobe, supplementary motor area, cingulate cortex and insula we

121 creases in rCBF were significantly higher in supplementary motor area, cingulate cortex, and dorsolat

122 tivation in the medial prefrontal cortex and supplementary motor area, cingulate gyrus, cuneus and oc

123 sk-related activation in regions such as the supplementary motor area, cingulate motor areas, premoto

124 otor cortex, premotor and prefrontal cortex, supplementary motor areas, cingulate sulcus, temporal lo

125 ngs showed abnormal primary motor cortex and supplementary motor area co-activation with increasing c

126 between the subthalamic nucleus and the pre-supplementary motor area contributing most strongly.

127 with temporo-parietal stroke integrated the supplementary motor area/dorsal anterior cingulate corte

128 observed increased activation in the insula, supplementary motor area, dorsolateral prefrontal cortex

129 ity between the right amygdala and the right supplementary motor area during both fearful versus neut

130 volving dorsal anterior cingulate cortex and supplementary motor area encoded the difference between

131 revealed that Broca's area and the left pre-supplementary motor area evoked distinct neural activity

132 Here, we studied pre-supplementary motor area F6 neurons with a task in which

133 vity between the left premotor area and left supplementary motor area, for both the left and the righ

134 Although the supplementary and pre-supplementary motor areas have been intensely investigat

135 pling increase of prefrontal cortex with the supplementary motor area, i.e. the mesial premotor loop.

136 (i) the mesial premotor loop comprising the supplementary motor area; (ii) the lateral premotor loop

137 uired from the parietal-occipital cortex and supplementary motor area in all subjects.

138 ary motor cortex in Tourette's syndrome, the supplementary motor area in Parkinson's disease, to vent

139 xels (>80%) at 3.0 T, with activation in the supplementary motor area in the 3.0-T data that was not

140 n primates indicating a critical role of the supplementary motor area in the organization of forthcom

141 control mechanism mediated by prefrontal and supplementary motor areas in PD with FOG.

142 in timing preferences (recently described in supplementary motor area) in an extensive network of top

143 e mesial frontocentral cortex (including the supplementary motor area) in the organization of sequent

144 Stimulation over the supplementary motor area induced accuracy errors only in

145 in the thalamus, anterior cingulate cortex, supplementary motor area, inferior parietal lobe, and do

146 re inversely associated with activity in the supplementary motor area, insula, and middle frontal gyr

147 al and lateral to the hand area, as well the supplementary motor area, insula, putamen, and cerebellu

148 Stimulation over the supplementary motor area interfered with the organizatio

149 r cortex (BA 4a), bilateral premotor cortex, supplementary motor area, intraparietal sulcus, dorsolat

150 ly, the connectivity between hippocampus and supplementary motor area is modulated by the similarity

151 d function (increased brain activity in left supplementary motor area, left parahippocampal gyrus, an

152 onization, including increased activation in supplementary motor area, left premotor area, right thal

153 ortex, bilateral medial frontal cortex, left supplementary motor area, left thalamus, left cerebellar

154 Abnormal anatomical connectivity of the supplementary motor area may contribute to the susceptib

155 t lateral prefrontal, insula, cingulate, and supplementary motor area network.

156 Finally, compared with the supplementary motor area, neurons in the presupplementar

157 vPPA), right temporal pole (sbvFTD) and left supplementary motor area (nfvPPA).

158 n GABA neurotransmitter concentration in the supplementary motor area of the human brain.

159 ex, the ventral lateral premotor cortex, the supplementary motor area on the medial wall, and the ros

160 value-related regions, only the ventral pre-supplementary motor area (or dorsal anterior cingulate c

161 feedback connections from putamen to the pre-supplementary motor area (Pcorrected = 0.020) and primar

162 We suggest that supplementary and pre-supplementary motor areas play a role in facilitating sp

163 medial part of PMC, putatively covering the supplementary motor area, plays a direct role in object

164 Inputs from the pre-supplementary motor area (pre-SMA) and inferior frontal

165 where thalamic neurons projecting to the pre-supplementary motor area (pre-SMA) are located relative

166 Here we provide evidence that the pre-supplementary motor area (pre-SMA) is causally involved

167 The pre-supplementary motor area (pre-SMA) plays a critical role

168 terior inferior frontal gyrus (pIFG) and pre-supplementary motor area (pre-SMA) with M1 at rest.

169 cture and functional connectivity of the pre-supplementary motor area (pre-SMA), assessed with magnet

170 d connectivity was directed from rIFG to pre-supplementary motor area (pre-SMA), indicating rIFG's do

171 ed with the accumulated gains, including pre-supplementary motor area (pre-SMA), inferior frontal gyr

172 by a higher increase in DA levels in the pre-supplementary motor area (pre-SMA).

173 re was an enhancement of activity in the pre-supplementary motor area (pre-SMA).

174 sal anterior cingulate cortex (dACC) and pre-supplementary motor area (pre-SMA).

175 eral prefrontal cortex (VLPFC) and the (pre)-supplementary motor area (pre-SMA/SMA) have dissociable

176 thought to be homologous to presupplementary/supplementary motor areas (pre-SMA/SMA) in humans, regio

177 us; and, (2) posterior cingulate cortex with supplementary motor area, precentral gyrus, and postcent

178 network, including the primary motor cortex, supplementary motor area, premotor area and superior par

179 in the regions of a cortical (motor cortex, supplementary motor area, premotor cortex) and subcortic

180 sing the putamen, caudate nucleus, thalamus, supplementary motor area, premotor cortex, and dorsolate

181 control and motivation to act, including the supplementary motor area, premotor cortex, primary motor

182 l previous monkey findings and show that the supplementary motor area, premotor, and the right prefro

183 f right inferior frontal cortex (r-IFC), pre-supplementary motor area (preSMA), and the subthalamic n

184 At voxel p < 0.05, FWE-corrected, the pre-supplementary motor area (preSMA), bilateral frontoparie

185 king, we recorded neurons from the human pre-supplementary motor area (preSMA), ventromedial prefront

186 on of effective connectivity between the pre-supplementary motor area, primary motor cortex and putam

187 or areas] and the medial motor cortex [MMCx; supplementary motor area proper (SMA), pre-SMA and foot

188 ment decision making and a posterior region (supplementary motor area proper) directly involved in mo

189 contrast, activation in dorsal striatum and supplementary motor areas reflects subjects' choice prob

190 et al. (2016) report that neurons in the pre-supplementary motor area represent the frequency of tact

191 Conversely, the supplementary motor area represents individual actions,

192 The supplementary motor area represents the anatomical link

193 rea, left ventral premotor cortex, posterior supplementary motor area, right superior part of the cer

194 ircuit and disconnection between the rostral supplementary motor area, rostral cingulate motor area a

195 ther with disconnections between the rostral supplementary motor area, rostral cingulate motor area a

196 o explore the neural changes associated with supplementary motor area rTMS in psychosis.

197 Akinesia is linked to hypoactivation of the supplementary motor area secondary to insufficient thala

198 a different region (medial frontal cortex, "supplementary motor area") showed greater activity durin

199 Task dependent BOLD activity in the supplementary motor area (SMA) and dorsolateral premotor

200 food cues in orbitofrontal cortex (OFC) and supplementary motor area (SMA) and less deactivation bel

201 mpal gyrus, with covarying reductions in the supplementary motor area (SMA) and orbitofrontal cortex.

202 ch as anterior cingulate and insular cortex, supplementary motor area (SMA) and parietal operculum (P

203 the dACC is selective for pain, whereas the supplementary motor area (SMA) and pre-SMA are specifica

204 The supplementary motor area (SMA) and pre-SMA are widely co

205 rupt profile change where the border between supplementary motor area (SMA) and pre-SMA is expected.

206 te nucleus (CN), cingulate motor area (CMA), supplementary motor area (SMA) and primary sensorimotor

207 ed by greater activation in the thalamus and supplementary motor area (SMA) and reduced connectivity

208 e during time perception including the right supplementary motor area (SMA) and right pre-SMA and bas

209 ed during simple manual movement, namely the supplementary motor area (SMA) and the cingulate motor a

210 Here we examined the connection between supplementary motor area (SMA) and the hand area of the

211 as on the medial wall of the hemisphere, the supplementary motor area (SMA) and the pre-SMA.

212 studies in normal humans have shown that the supplementary motor area (SMA) and the primary motor cor

213 of spinal termination of efferents from the supplementary motor area (SMA) and the two caudal cingul

214 erent parts of primary motor cortex (M1) and supplementary motor area (SMA) bilaterally were assessed

215 ing across the primary motor cortex (M1) and supplementary motor area (SMA) by inspecting the positiv

216 inferior frontal, inferior premotor, insula, supplementary motor area (SMA) complex, striatum, and st

217 Neural signals in the supplementary motor area (SMA) correlate with the intens

218 at pre-movement alpha oscillations in M1 and supplementary motor area (SMA) correlated with agency ra

219 ogram (EEG) over motor, pre-motor cortex and supplementary motor area (SMA) during action observation

220 eft dorsolateral prefrontal cortex (PFC) and supplementary motor area (SMA) during emotion regulation

221 oscillations significantly increased in the supplementary motor area (SMA) during post-training comp

222 ivity of the primary motor cortex and caudal supplementary motor area (SMA) during volitional movemen

223 nce of basal ganglia, prefrontal cortex, and supplementary motor area (SMA) for timing.

224 Activity in the supplementary motor area (SMA) has been associated with

225 ility.SIGNIFICANCE STATEMENT The role of the supplementary motor area (SMA) in initiating movement re

226 ential studies in man suggest a role for the supplementary motor area (SMA) in movement preparation,

227 The supplementary motor area (SMA) is believed to contribute

228 The supplementary motor area (SMA) is frequently involved by

229 The supplementary motor area (SMA) makes a crucial contribut

230 tivity of individual neurons recorded in the supplementary motor area (SMA) of monkeys during a seria

231 dies in man have identified the premotor and supplementary motor area (SMA) of the cortex as being of

232 We recorded from the supplementary motor area (SMA) of two monkeys as they ex

233 We determined that the supplementary motor area (SMA) plays an important role i

234 and premotor cortex bilaterally, also in the supplementary motor area (SMA) predominantly in the left

235 e right dorsal premotor cortex (rPMd) or the supplementary motor area (SMA) prior to the TS at variou

236 y processing risk costs and midcingulate and supplementary motor area (SMA) processing effort costs.

237 uted pattern; more extensive activity in the supplementary motor area (SMA) proper that extended into

238 In contrast, M1 and supplementary motor area (SMA) showed more integrative s

239 Here we report neuronal activity in the supplementary motor area (SMA) that is correlated with b

240 The contribution of the supplementary motor area (SMA) to movement initiation re

241 ections from the digit representation in the supplementary motor area (SMA) to the PMd and PMv are st

242 the basal ganglia, motor cortex area 4, and supplementary motor area (SMA) using functional magnetic

243 prising M1, lateral premotor cortex, and the supplementary motor area (SMA) were assessed using dynam

244 tor area (PMD), ventral premotor area (PMV), supplementary motor area (SMA), and frontal eye field (F

245 tor area (PMD), ventral premotor area (PMV), supplementary motor area (SMA), and frontal eye field (F

246 l cortex, the supplementary eye field (SEF), supplementary motor area (SMA), and pre-SMA have been im

247 e dorsal oculomotor area (OMD; area 8b), the supplementary motor area (SMA), and somatosensory cortex

248 1), injected isotope tracers into M1 and the supplementary motor area (SMA), and studied projections

249 in neuronal firing rate, particularly in the supplementary motor area (SMA), as the reported time of

250 OLD response than did heavy drinkers in left supplementary motor area (SMA), bilateral parietal lobul

251 ions with the primary motor cortex (M1), the supplementary motor area (SMA), cingulate motor areas, s

252 motor cortex (M1), premotor cortex (PM), the supplementary motor area (SMA), cortex on the medial wal

253 ctivity between the primary motor area (M1), supplementary motor area (SMA), dorsal premotor cortex (

254 Activations within the supplementary motor area (SMA), frontal operculum, middl

255 he primary somatosensory cortex (S1) and the supplementary motor area (SMA), in both patient populati

256 y when the actions are familiar; and (2) the supplementary motor area (SMA), involved in active motor

257 number of frontal areas, including the left supplementary motor area (SMA), left dorsal premotor cor

258 educed activation across both trial types in supplementary motor area (SMA), middle temporal gyrus an

259 atterned neural time-keeping activity in the supplementary motor area (SMA), orchestrated and sequenc

260 ith the "timing network" (TN), including the supplementary motor area (SMA), precentral gyrus, and ri

261 MDr) divisions, ventral premotor area (PMV), supplementary motor area (SMA), presupplementary motor a

262 medial premotor system, including the caudal supplementary motor area (SMA), the left putamen, and th

263 ter connectivity between the putamen and the supplementary motor area (SMA), the premotor cortex (PMC

264 thalamus (THAL), ventral-striatum (VS), and supplementary motor area (SMA), using both mediator anal

265 tional connectivity with the striatum is the supplementary motor area (SMA), where we applied tSMS.

266 that, if an individual has more GABA in the supplementary motor area (SMA)--a region previously asso

267 onstrate that GABA concentrations within the supplementary motor area (SMA)--a region strongly associ

268 ed rCBF change in the thalamus, midbrain and supplementary motor area (SMA).

269 ions were found in the contralateral PMv and supplementary motor area (SMA).

270 (M1), primary somatosensory cortex (S1), and supplementary motor area (SMA).

271 sly recorded pairs of neurons in the macaque supplementary motor area (SMA).

272 sensory area (S1), premotor cortex (PMC) and supplementary motor area (SMA).

273 ck to the cerebral cortex, in particular the supplementary motor area (SMA).

274 , parietal and paracingulate cortex, and the supplementary motor area (SMA).

275 portion of area 46, area ProM, CMAr, and the supplementary motor area (SMA).

276 tional significant increases in the anterior supplementary motor area (SMA)/cingulate.

277 or subdivision of medial frontal cortex [pre-supplementary motor area (SMA)] was activated, which cou

278 tralateral thalamus, ipsilateral cerebellum, supplementary motor area (SMA)]; however, the TD group s

279 resting motor network between right and left supplementary motor areas (SMA) was elevated after train

280 n the right dorso-lateral prefrontal cortex, supplementary motor areas (SMA), the right premotor area

281 ons) located on the right medial wall in the supplementary motor area ('SMA proper').

282 we show that in the medial premotor cortex (supplementary motor area [SMA]) of the human brain, neur

283 ortices (hereafter, referred to as hand-M1), supplementary motor areas (SMAs), premotor cortices (PMC

284 nterest: the prefrontal cortex, motor cortex/supplementary motor area, somatosensory cortex, temporal

285 These regions as well as supplementary motor area, striatum and the hippocampus h

286 cortex and medial caudate nucleus and 2) the supplementary motor area, superior medial frontal cortex

287 s such as medial superior frontal gyrus (pre-supplementary motor area/supplementary eye field), dorso

288 ateral STG, precentral and postcentral gyri, supplementary motor area, supramarginal gyrus, posterior

289 eased activation in a smaller cluster in the supplementary motor area survived comparison with the ps

290 resentation in the primary motor cortex; the supplementary motor area; the inferior lateral premotor

291 fluence from the right amygdala to the right supplementary motor area to happy stimuli (P < 0.05) wit

292 two components in dorsal premotor cortex and supplementary motor areas, two regions that may be impor

293 furthermore, the increased activation in the supplementary motor area was abuse specific.

294 on circuit in the superior parietal lobe and supplementary motor area was activated in response to th

295 r insula and the presupplementary motor area/supplementary motor area was associated with a greater d

296 dorsal and ventral premotor cortex) and the supplementary motor area was compared between groups (co

297 les, including a left inferior frontal gyrus/supplementary motor area, which was most strongly connec

298 g task blocks was present in the caudate and supplementary motor area, while sustained negative activ

299 Coactivation in the motor cortex and supplementary motor area with increasing cognitive load

300 ected) in the left premotor cortex and right supplementary motor area, with concomitant reduction in